Cas 1397692-33-9,(5S,6S,7R,8S,10S)-ethyl 8-hydroxy-7-methyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]decane-6-carboxylate

1397692-33-9

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Basic information

Product Name: (5S,6S,7R,8S,10S)-ethyl 8-hydroxy-7-methyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]decane-6-carboxylate
Synonyms: (5S,6S,7R,8S,10S)-ethyl 8-hydroxy-7-methyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]decane-6-carboxylate
CAS NO:1397692-33-9
Molecular Formula:
Molecular Weight: 379.501
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (5S,6S,7R,8S,10S)-ethyl 8-hydroxy-7-methyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]decane-6-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (5S,6S,7R,8S,10S)-ethyl 8-hydroxy-7-methyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]decane-6-carboxylate(1397692-33-9)
EPA Substance Registry System: (5S,6S,7R,8S,10S)-ethyl 8-hydroxy-7-methyl-4-oxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]decane-6-carboxylate(1397692-33-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1397692-33-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1397692-33-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,7,6,9 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1397692-33:
(9*1)+(8*3)+(7*9)+(6*7)+(5*6)+(4*9)+(3*2)+(2*3)+(1*3)=219
219 % 10 = 9
So 1397692-33-9 is a valid CAS Registry Number.

1397692-33-9Upstream product

1397692-29-3 (5S,6S,7R,10S)-ethyl 7-methyl-4,8-dioxo-10-phenyl-2-thioxo-1-thia-3-azaspiro[4.5]decane-6-carboxylate

1397692-33-9Downstream Products

1397692-33-9Relevant academic research and scientific papers

Asymmetric construction of spirocyclohexanonerhodanines catalyzed by simple diamine derived from chiral tert-leucine

Wu, Wenbin,Huang, Huicai,Yuan, Xiaoqian,Zhu, Kailong,Ye, Jinxing

supporting information; experimental part, p. 9180 - 9182 (2012/09/22)

A diamine-catalyzed asymmetric tandem reaction between α,β- unsaturated ketones and rhodanine derivatives has been developed to synthesize various spirocyclic compounds with high stereoselectivities (up to 99% ee and >20:1 dr). The products obtained contain two pharmaceutically relevant features: the biologically active rhodanine moiety embedded in a spirocyclic unit.

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